Serum tryptase level is a better predictor of systemic side effects than prostaglandin D2 metabolites during venom immunotherapy in children

Objectives: we performed a prospective study to analyze mast cell mediators as predictors of systemic adverse reactions during rush venom-specifi c immunotherapy (vit) in children. patients and methods: nineteen children aged 5-17 years received vit with venomenhal (halallergy). we analyzed serum tryptase (cap,phadia),plasma prostaglandin (pg) d2 metabolites (9α,11ß-pgf2),and urine pgd2 metabolites (9α,11ß-pgf2,tetranor-pgd-m) using gas chromatography mass spectrometry before and after the rush protocol. results: three boys with high baseline serum tryptase values (>7.76 μg/l) (p<.001) and low 9α,11ß-pgf2 concentrations developed grade iii systemic adverse reactions during vit. baseline serum tryptase was lowest in children who had a mueller grade ii reaction (1.93 [0.36]) before vit and highest in children with a mueller grade iii reaction (6.31 [4.80]) (p=.029). repeated measures analysis of variance confi rmed that,in children who developed systemic adverse reactions during vit,serum tryptase was higher both before and after desensitization and increased signifi cantly following the procedure. analysis of pgd2 metabolites in the prediction of systemic adverse reactions during vit was inadequate (sensitivity 67% and specifi city 0.53%),whilst prediction based on serum tryptase was accurate. conclusions: in children with severe systemic adverse reactions to hymenoptera sting,the evaluation of baseline tryptase levels should be a standard procedure. children with apis mellifera venom allergy and baseline tryptase levels higher than 7.75 μg/l are at risk of anaphylaxis during buildup. lower baseline values of plasma and urinary pgd2 metabolite concentration in patients with systemic adverse reaction during vit suggest that prostaglandin catabolism is altered.© 2011 esmon publicidad.